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Plos One|April 18, 2013
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery diseaseAdriana Huertas-Vazquez, Christopher P Nelson, Xiuqing Guo, et al.Nature Aging|April 28, 2023
Measurement and initial characterization of leukocyte telomere length in 474,074 participants in UK BiobankV Codd, M Denniff, C Swinfield, et al.Circulation|October 7, 2017
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide SignalingConnor A Emdin, Amit V Khera, Derek Klarin, et al.Nature Communications|November 24, 2018
Molecular insights into genome-wide association studies of chronic kidney disease-defining traitsXiaoguang Xu, James M Eales, Artur Akbarov, et al.Hypertension (Dallas, Tex. : 1979)|March 13, 2013
Genetic predisposition to higher blood pressure increases coronary artery disease riskWolfgang Lieb, Henning Jansen, Christina Loley, et al.Diabetes|November 4, 2018
DNA Sequence Variation in ACVR1C Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 DiabetesConnor A Emdin, Amit V Khera, Krishna Aragam, et al.Atherosclerosis|August 8, 2009
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery diseasePatrick Linsel-Nitschke, Jörg Heeren, Zouhair Aherrahrou, et al.International Journal of Cardiology|January 8, 2018
Fibroblast growth factor 23 is related to profiles indicating volume overload, poor therapy optimization and prognosis in patients with new-onset and worsening heart failureJozine M Ter Maaten, Adriaan A Voors, Kevin Damman, et al.European Journal of Heart Failure|April 4, 2020
A network analysis to identify pathophysiological pathways distinguishing ischaemic from non-ischaemic heart failureIziah E Sama, Rebecca J Woolley, Jan F Nauta, et al.Circulation. Genomic and Precision Medicine|September 1, 2020
Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery DiseaseAkihiro Nomura, Connor A Emdin, Hong Hee Won, et al.Pageof 67